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Development of EGFP-Expressing Cell Line for Biocompatibility Evaluation of Osteoinductive CaP Ceramics

机译:表达EGFP表达细胞系的骨诱导帽陶瓷的生物相容性评价

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This study investigated the utility of genetically modified cell line for fast and non-destructive cytotoxicity evaluation of biomaterials. The EGFP(enhanced green fluorescence protein)-expressing plasmid pcDNA-EGFP was constructed, and electroporated into ROS 17/28 osteoblastic cells to generate an EGFP-labeled stable cell line, ROS-EGFP. This genetically modified cell line provided two unique opportunities to qualitative and semi-quantitative evaluation of cell growth on biomaterials without destruction of samples. Firstly, utilizing the fluorescence of EGFP expressed in the cells, the viability state of cells on biomaterials was evaluated using a fluorescent light microscope. Secondly, the proliferation of cells on biomaterials, which was identified by MTT assay, was demonstrated according to the microscopically counted fluorescent cell numbers. From the results, it could be concluded that the ROS-EGFP cell line was an effective tool to trace the fate of cells on biomaterials and to evaluate the biocompatibility of biomaterials to cell growth in vitro.
机译:本研究研究了遗传修饰细胞系对生物材料的快速和非破坏性细胞毒性评价的效用。构建EGFP(增强的绿色荧光蛋白) - 抑制质粒pCDNA-EGFP,并将其电穿孔到ROS 17/28骨细胞中,以产生EGFP标记的稳定细胞系ROS-EGFP。该基因改性的细胞系为生物材料对细胞生长的定性和半定量评估提供了两个独特的机会,而不会破坏样品。首先,利用细胞中表达的EGFP的荧光,使用荧光显微镜评估生物材料上的细胞的活力状态。其次,根据显微透视计数的荧光细胞数来证明通过MTT测定鉴定的生物材料上的细胞的增殖。从结果中,可以得出结论,ROS-EGFP细胞系是追踪生物材料对细胞的命运的有效工具,并评估生物材料的生物相容性在体外进行细胞生长。

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